NANOVIS® Corporate News

Carmel, Ind. (September 22, ) – Nanovis Spine, LLC (Nanovis) announced today that it has received U.S. Food and Drug Administration (FDA) 510(k) clearance of the company’s sterile packed FortiCore® interbody fusion devices. Unlike conventional implants comprising PEEK or sprayed titanium coating, FortiCore® implants have the benefits of a highly porous titanium scaffold engineered for strong, durable integration with a PEEK core.

Success and market share in the slow-growing, crowded spinal sector are dependent upon differentiated solutions supported by clinical evidence.

It seemed, at first, like a routine sack. Dallas Cowboys quarterback Tony Romo was scram- bling outside the pocket to his left, looking frenziedly for an open receiver, when he stepped into a slide to avoid a tackle. It didn’t work.

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